Functional Neuroimaging of Postural Reconstruction

This study has been completed.
Sponsor:
Information provided by:
University Hospital, Strasbourg, France
ClinicalTrials.gov Identifier:
NCT01013727
First received: November 13, 2009
Last updated: April 28, 2010
Last verified: April 2010
  Purpose

To study in two cross-sections of healthy volunteers, with single photon emission computed tomography (SPECT), the possible changes generated in the mid-term by two rehabilitation techniques: the postural reconstruction and the muscular stretching. The changes in the cortical activation patterns will be estimated during a non-specific position of the ankle, held static.

The influence of each technique will be estimated though the evidence of a change in the functional mapping of the areas activated during the defined motor task on healthy volunteers.


Condition Intervention
Healthy
Radiation: SPECT : ECD-Tc99m - Neurolite, Bristol-Myers Squibb Medical Imaging

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Official Title: Functional Neuroimaging of Postural Reconstruction: Preliminary Study on a Dorsiflexion Motion of the Ankle and Comparison Between an Arm Following Postural Reconstruction Program and a Comparator Arm Following a Muscular Stretching Program

Resource links provided by NLM:


Further study details as provided by University Hospital, Strasbourg, France:

Primary Outcome Measures:
  • Change in the functional mapping of the areas activated during the defined motor task on healthy volunteers. [ Time Frame: 8 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 16
Study Start Date: November 2009
Study Completion Date: April 2010
Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Postural Reconstruction Radiation: SPECT : ECD-Tc99m - Neurolite, Bristol-Myers Squibb Medical Imaging
Active Comparator: muscular stretching Radiation: SPECT : ECD-Tc99m - Neurolite, Bristol-Myers Squibb Medical Imaging

Detailed Description:

This is a monocentre, randomized study.

  Eligibility

Ages Eligible for Study:   18 Years to 35 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • male or female 18 to 35 years old

Exclusion Criteria:

  • pregnant, lactating
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01013727

Locations
France
University Hospital Strasbourg
Strasbourg, France, 67000
Sponsors and Collaborators
University Hospital, Strasbourg, France
Investigators
Principal Investigator: Izzie Jacques Namer, Md University Hospital, Strasbourg, France
  More Information

No publications provided

Responsible Party: Christine GEILLER directeur de la DRCI, University Hospital, Strasbourg, France
ClinicalTrials.gov Identifier: NCT01013727     History of Changes
Other Study ID Numbers: 4551
Study First Received: November 13, 2009
Last Updated: April 28, 2010
Health Authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

Keywords provided by University Hospital, Strasbourg, France:
Volunteers
healthy subjects

ClinicalTrials.gov processed this record on April 15, 2014